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早产儿储存前白细胞滤除的红细胞输注中的细胞因子负荷

Cytokine load in prestorage leukoreduced PRBC transfusions in premature infants.

作者信息

Locke Robert, Paul David, Touch Suzanne, Mackley Amy, Maduskuie Victoria, Fawcett Paul

机构信息

Division of Neonatology, Christiana Hospital, Newark, DE, USA.

出版信息

J Perinatol. 2005 Aug;25(8):526-30. doi: 10.1038/sj.jp.7211340.

Abstract

OBJECTIVE

Despite the high frequency of packed red blood cell (PRBC) transfusions given to premature neonates, there has been no previous investigation in this population to determine whether small-volume PRBC transfusions using prestorage leukoreduction techniques (1) provide a cytokine load in the transfusate and (2) if there is a load, whether that load alters serum cytokine levels after transfusion.

STUDY DESIGN

In all, 27 PRBC units, which were leukoreduced at the time of donation, were followed for cytokine analysis for the duration of the unit's shelf life (1 to 42 days). Infants who received transfusion from these units had cytokines measured pre and post-transfusion.

RESULTS

There were no significant levels of interleukin 6 (IL-6), interleukin 10 (IL-10), interleukin 1 beta (IL-1beta), or human tumor necrosis factor alpha (TNF-alpha) detected during the storage time period. Nine premature infants who received transfusions from these units had serum cytokines levels measured pre- vs post-PRBC transfusion, with no evidence of alterations (IL-6 p=0.51, IL-10 p=0.10, IL-1beta p=0.44, TNF-alpha p=0.86).

CONCLUSIONS

The determination of a nondetectable or very low level of a cytokine load contained within the PRBC transfusate, combined with the absence of evidence of an in vivo cytokine effect, is important in establishing the safety profile for PRBC blood-banking methods used with premature neonates.

摘要

目的

尽管给早产儿输注浓缩红细胞(PRBC)的频率很高,但此前尚未对该人群进行过研究,以确定使用储存前白细胞滤除技术进行的小剂量PRBC输注是否(1)在输注液中产生细胞因子负荷,以及(2)如果存在负荷,该负荷是否会在输血后改变血清细胞因子水平。

研究设计

总共对27个在献血时进行了白细胞滤除的PRBC单位进行了跟踪,在单位的保质期(1至42天)内进行细胞因子分析。接受这些单位输血的婴儿在输血前后测量细胞因子。

结果

在储存期间未检测到显著水平的白细胞介素6(IL-6)、白细胞介素10(IL-10)、白细胞介素1β(IL-1β)或人肿瘤坏死因子α(TNF-α)。9名接受这些单位输血的早产儿在PRBC输血前后测量了血清细胞因子水平,没有变化的证据(IL-6 p = 0.51,IL-10 p = 0.10,IL-1β p = 0.44,TNF-α p = 0.86)。

结论

确定PRBC输注液中细胞因子负荷不可检测或非常低的水平,以及缺乏体内细胞因子效应的证据,对于建立用于早产儿的PRBC血库方法的安全性概况很重要。

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